Impact of Interleukin 28B (rs12979860) Genotype on Virological Responses Chronic Hepatitis C Treatment
Primary Purpose
Hepatitis C, Hepatitis C Relapse
Status
Completed
Phase
Phase 3
Locations
Pakistan
Study Type
Interventional
Intervention
Pegylated Interferon α2
Ribavirin
Sponsored by
About this trial
This is an interventional treatment trial for Hepatitis C focused on measuring HCV genotype 2, HCV genotype 3, IL-28B, PEG-INF.
Eligibility Criteria
Inclusion Criteria:
- patients with diagnosis of chronic hepatitis C genotype 2 or 3
Exclusion Criteria:
- Patients with hepatitis genotype I and IV
Sites / Locations
- Muhammad Zafar Majeed Babar
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
chronic hepatitis C genotype 2 or 3
Arm Description
In all patients Pegylated Interferon α2 (pegIFN) plus Ribavirin were given in standard doses. Peg-INF was given in a dose of 180 μg/week and ribavirin 1200 mg/day to every patient for the period of 24 weeks for HCV genotype 2 & 3
Outcomes
Primary Outcome Measures
Treatment Success rate
Treatment Success rate (End Treatment Response) was noted to check the adequency of treatment
Secondary Outcome Measures
Sustained Virological Response
Sustained Virological Response was noted to check treatment success after extended period
Relapse Rate
Relapse Rate to check re-occurrence of Hepatitis infection
Full Information
NCT ID
NCT03090035
First Posted
February 27, 2017
Last Updated
April 22, 2017
Sponsor
Sheikh Zayed Medical College
1. Study Identification
Unique Protocol Identification Number
NCT03090035
Brief Title
Impact of Interleukin 28B (rs12979860) Genotype on Virological Responses Chronic Hepatitis C Treatment
Official Title
Impact of Interleukin 28B (rs12979860) Genotype on Virological Responses in Chronic Hepatitis C Treatment
Study Type
Interventional
2. Study Status
Record Verification Date
April 2017
Overall Recruitment Status
Completed
Study Start Date
January 1, 2014 (Actual)
Primary Completion Date
July 1, 2014 (Actual)
Study Completion Date
December 31, 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sheikh Zayed Medical College
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Objective:
Pegulated Interferon α2 plus ribavirin is a treatment of choice in patients with chronic hepatitis C infection. This study was conducted to find out the frequency of different IL-28B (rs12979860) genotypes in patients with chronic hepatitis C (HCV genotype type 2 & 3) infection treated with Pegulated Interferon α2 plus ribavirin and to evaluate the role of IL-28B genotypes in achieving Sustained Virological Response (SVR).
Methods:
In this non-randomized observational study, ninety eight (98) patients with diagnosis of chronic hepatitis C were included. In all patients, Peg-IFN plus Ribavirin were given in standard doses for 24 weeks. End treatment response, sustained virological response, and relapse rate were the primary endpoints of this study. Analysis of IL28B (rs12979860) polymorphism (CC, CT and TT) was performed by PCR-RFLP protocol.
Detailed Description
INTRODUCTION:
Hepatitis C virus (HCV) is a major health problem that effects nearly 170 million people worldwide [1, 2]. According to a report, about 64-103 million people are suffering from chronic HCV infection [3] and this chronic infection results in liver scarring, hepatocellular carcinoma or end-stage liver disease in about forty thousand (40,000) patients every year [4, 5]. According to WHO, liver disease initiated by chronic hepatitis C infection is responsible for more than 35 thousand deaths and 3 to 4 million people are infected every year[3, 6]. Hepatitis C Virus has been classified into seven genotypes and several subtypes, which are associated with distinct forms of geographic dispersal [7, 8]. The success of HCV treatment is affected by many viral, treatment or host factors.
Pegulated Interferon α2 plus ribavirin is a treatment of choice in patients with chronic hepatitis C infection. Sustained virological response (SVR) rate with this treatment in HCV-2 & 3 has been reported to be 58-84% in previously untreated patients [9]. SVR can be affected by liver cirrhosis, hepatocellular carcinoma, ethnicity, age, gender and obesity. [10, 11] It has been clarified by some studies that interleukin-28B has an important role in the treatment success of HCV infection and IL-28B CC genotype is associated with 2 folds higher sustained virological response (SVR) as compared to CT and TT genotype [12-14]. The aim of present study was to find out the frequency of different IL28B (rs12979860) genotypes in patients with chronic hepatitis C (genotype type 2 or 3) infection treated with Pegulated Interferon α2 plus ribavirin and to evaluate the role of IL-28B genotypes in achieving Sustained Virological Response (SVR).
METHODS:
This non-randomized observational study was conducted in Sheikh Zayed Medical College/Hospital Rahim Yaar Khan. A total of ninety eight (98) patients with diagnosis of chronic hepatitis C genotype 2 or 3 were involved in this study. The duration of study was from January 2015 to January 2016. People living in Rahim Yaar Khan City belongs to different ethinic backgrounds because this city is located at the junction of three provinces of Pakistan (total provinces are four), so people residing here represent the whole Pakistani population living in different provinces. Institutional ethical approval was taken before starting this research work. A written informed consent was taken from every patient before including him/her in this study.
The diagnosis of chronic hepatitis C was made through liver enzyme levels, HCV-RNA positivity and anti-HCV antibody test. Patients with other chronic liver disorders, with positive hepatitis B virus (HBV), and human immunodeficiency virus (HIV) infection were excluded from this study.
Treatment Protocol and Detection of IL28B Polymorphism:
In all patients Pegulated Interferon α2 (pegIFN) plus Ribavirin were given in standard doses. PegINF was given in a dose of 180 μg/week and ribavirin 1200 mg/day to every patient for the period of 24 weeks for HCV genotype 2 & 3.
PCR analysis was done in every patient before starting the treatment, after 24 weeks of treatment (to see end treatment response) and 48 weeks (to evaluate SVR and relapse rate) of treatment. Analysis of IL28B (rs12979860) polymorphism (CC, CT and TT) was performed by PCR restriction fragment length polymorphism (RFLP) assay protocol. Pyrosequencing method was used to determine HCV genotypes.
Data analysis was done using SPSS V17 software. Mean and standard deviation were used for the presentation of quantitative variables. Frequency and percentages were used to present qualitative data. Chi-square test/Fisher Exact test was used to compare qualitative data. P-value <0.05 was taken as significant.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatitis C, Hepatitis C Relapse
Keywords
HCV genotype 2, HCV genotype 3, IL-28B, PEG-INF.
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Model Description
Clinical trial
Masking
None (Open Label)
Allocation
N/A
Enrollment
98 (Actual)
8. Arms, Groups, and Interventions
Arm Title
chronic hepatitis C genotype 2 or 3
Arm Type
Experimental
Arm Description
In all patients Pegylated Interferon α2 (pegIFN) plus Ribavirin were given in standard doses. Peg-INF was given in a dose of 180 μg/week and ribavirin 1200 mg/day to every patient for the period of 24 weeks for HCV genotype 2 & 3
Intervention Type
Drug
Intervention Name(s)
Pegylated Interferon α2
Other Intervention Name(s)
Unipg
Intervention Description
Peg-INF was given in a dose of 180 μg/week
Intervention Type
Drug
Intervention Name(s)
Ribavirin
Other Intervention Name(s)
Ribavil
Intervention Description
ribavirin 1200 mg/day to every patient for the period of 24 weeks for HCV genotype 2 & 3
Primary Outcome Measure Information:
Title
Treatment Success rate
Description
Treatment Success rate (End Treatment Response) was noted to check the adequency of treatment
Time Frame
after 24 weeks of treatment
Secondary Outcome Measure Information:
Title
Sustained Virological Response
Description
Sustained Virological Response was noted to check treatment success after extended period
Time Frame
After 48 weeks of treament
Title
Relapse Rate
Description
Relapse Rate to check re-occurrence of Hepatitis infection
Time Frame
After 48 weeks of treament
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
patients with diagnosis of chronic hepatitis C genotype 2 or 3
Exclusion Criteria:
Patients with hepatitis genotype I and IV
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Muhammad ZM Babar, FCPS
Organizational Affiliation
Sheikh Zayed Medical College/Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Muhammad Zafar Majeed Babar
City
Sadiqabad
State/Province
Punjab
ZIP/Postal Code
64200
Country
Pakistan
12. IPD Sharing Statement
Plan to Share IPD
No
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Impact of Interleukin 28B (rs12979860) Genotype on Virological Responses Chronic Hepatitis C Treatment
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